Methanol → 3-Hydroxy-2-phenethyl-5,6-dimethoxy-2,3-dihydro-1H-isoindol-1-one

HRID 65691

反応式

HRID 65691 の反応式
[BH4-].[K+].[CH3:3][O:4][C:5]1[CH:6]=[C:7]2[C:12](=[O:13])[N:11]([CH2:14][CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:9](=[O:10])[C:8]2=[CH:22][C:23]=1[O:24][CH3:25].O1CCOCC1.CO>O>[OH:13][CH:12]1[C:7]2[C:8](=[CH:22][C:23]([O:24][CH3:25])=[C:5]([O:4][CH3:3])[CH:6]=2)[C:9](=[O:10])[N:11]1[CH2:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

6

反応物 4

HCID 887MethanolHCID 312751,4-DioxaneHCID 4192641Potassium borohydrideHCID 227575535,6-Dimethoxy-2-(2-phenylethyl)-1H-isoindole-1,3(2H)-dione

生成物 1

HCID 227575543-Hydroxy-2-phenethyl-5,6-dimethoxy-2,3-dihydro-1H-isoindol-1-one収率 96.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Potassium borohydride (4.87 g) dissolved in distilled water (58.7 cc) is added to 4,5-dimethoxy-N-phenethyl phthalimide (28 g) suspended in a mixture (180 cc) consisting of equal volumes of dioxan and methanol. The reaction mixture is heated under reflux for 2 hours and then concentrated to a volume of 60 cc and distilled water (450 cc) is added. After cooling, the resulting precipitate is filtered off, washed three times with distilled water (total 1000 cc) and dried under reduced pressure (20 mm Hg) at 25° C. 3-Hydroxy-2-phenethyl-5,6-dimethoxy-2,3-dihydro-1H-isoindol-1-one (27.3 g), melting at 130° C., is thus obtained.

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for 2 hours
  3. concentrationconcentrated to a volume of 60 cc
  4. distillationdistilled water (450 cc)
  5. additionis added
  6. temperatureAfter cooling
  7. filtrationthe resulting precipitate is filtered off
  8. washwashed three times with distilled water (total 1000 cc)
  9. customdried under reduced pressure (20 mm Hg) at 25° C

出典と根拠

ORDレコード
ord-8df3739a1b454da3873c39b824b653b5
出典データセット
uspto-grants-1978_12
特許番号
US04128650

関連ノート

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